000 01367 a2200397 4500
005 20250517152031.0
264 0 _c20180827
008 201808s 0 0 eng d
022 _a1473-5717
024 7 _a10.1097/MCD.0000000000000182
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBayat, Allan
245 0 0 _aFamilial craniofacial abnormality and polymicrogyria associated with a microdeletion affecting the NFIA gene.
_h[electronic resource]
260 _bClinical dysmorphology
_cJul 2017
300 _a148-153 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aChild
650 0 4 _aChromosome Deletion
650 0 4 _aChromosome Mapping
650 0 4 _aCraniofacial Abnormalities
_xdiagnosis
650 0 4 _aFacies
650 0 4 _aFemale
650 0 4 _aGenetic Association Studies
650 0 4 _aHigh-Throughput Nucleotide Sequencing
650 0 4 _aHumans
650 0 4 _aMagnetic Resonance Imaging
650 0 4 _aNFI Transcription Factors
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPolymicrogyria
_xdiagnosis
700 1 _aKirchhoff, Maria
700 1 _aMadsen, Camilla G
700 1 _aRoos, Laura
700 1 _aKreiborg, Sven
773 0 _tClinical dysmorphology
_gvol. 26
_gno. 3
_gp. 148-153
856 4 0 _uhttps://doi.org/10.1097/MCD.0000000000000182
_zAvailable from publisher's website
999 _c27123040
_d27123040